Variant report

Variant rs12001067
Chromosome Location chr9:139672195-139672196
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139668200-139682400 Weak transcription Right Atrium heart
2 chr9:139670800-139673400 Enhancers Fetal Intestine Large intestine
3 chr9:139671200-139672600 Enhancers Duodenum Mucosa Duodenum
4 chr9:139671200-139672600 Enhancers K562 blood
5 chr9:139671400-139672400 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:139671400-139672400 Flanking Active TSS HepG2 liver
7 chr9:139671400-139672600 Enhancers Placenta Amnion Placenta Amnion
8 chr9:139671600-139672400 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr9:139671600-139672400 Flanking Active TSS Rectal Mucosa Donor 31 rectum
10 chr9:139671600-139672600 Enhancers Sigmoid Colon Sigmoid Colon
11 chr9:139671800-139672200 Flanking Active TSS Colonic Mucosa Colon
12 chr9:139671800-139672200 Flanking Active TSS Fetal Intestine Small intestine
13 chr9:139672000-139672200 Enhancers Rectal Mucosa Donor 29 rectum
14 chr9:139672000-139672600 Enhancers Placenta Placenta

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